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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Anhydride → N-(4,6-Dichloropyrimidin-2-yl)formamide

HRID 1730143
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HRID 1730143 반응식
[NH2:1][C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[N:3]=1.[C:10](OC(=O)C)(=[O:12])C>C(O)=O>[CH:10]([NH:1][C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[N:3]=1)=[O:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic Anhydride2회HCID 655222-Amino-4,6-dichloropyrimidine

생성물 1

HCID 21499405N-(4,6-Dichloropyrimidin-2-yl)formamide수율 77%

시약·촉매·용매 1

HCID 284Formic Acid용매

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온도
50 °C

실험 절차

A 250 ml. three necked flask was fitted with a mechanical stirrer, a thermometer, and a reflux condenser with drying tube. To the flask was charged 70 ml. of a 98% formic acid and 3.85 g (0.025 mole) of 2-amino-4,6-dichloropyrimidine as prepared in example 1. Acetic anhydride, 30 ml. was added slowly with stirring to maintain temperature below 50° C. When the addition of acetic anhydride was complete, the mixture was heated for 6 more hours at 50° C and then allowed to stand overnight at room temperature. Excess formic acid and acetic anhydride were evaporated under vacuum. The solid residue was crystallized from 15 ml. of ethyl alcohol. There was obtained 3.7 g of 2-formamido-4,6-dichloropyrimidine (PY-24) in the form of white crystals, melting point, 142°-144° C, yield 77%.

후처리

  1. customthree necked flask was fitted with a mechanical stirrer
  2. customa thermometer, and a reflux condenser with drying tube
  3. additionTo the flask was charged 70 ml
  4. additionwas added slowly
  5. temperatureto maintain temperature below 50° C
  6. customExcess formic acid and acetic anhydride were evaporated under vacuum
  7. customThe solid residue was crystallized from 15 ml

출처 및 근거

ORD 기록
ord-38f04e15867449d794363b319ec721e0
출처 데이터셋
uspto-grants-1976_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03991190

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