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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → cis 4-Thiocyanatomethyl-3-amino-2-oxo-azetidine hydrochloride

HRID 345650
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HRID 345650 반응식
[S:1]([CH2:4][C@H:5]1[NH:8][C:7](=[O:9])[C@H:6]1[N:10]1C(=O)C2=CC=CC=C2C1=O)[C:2]#[N:3].O.NN.[ClH:24]>O1CCOCC1>[ClH:24].[S:1]([CH2:4][C@H:5]1[NH:8][C:7](=[O:9])[C@H:6]1[NH2:10])[C:2]#[N:3]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 24654Hydrazine hydrate (1:1)HCID 86743759cis 4-Thiocyanatomethyl-3-phthalimido-2-oxo-azetidine

생성물 1

HCID 86743760cis 4-Thiocyanatomethyl-3-amino-2-oxo-azetidine hydrochloride

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
20 °C

실험 절차

A hot mixture of 1.45 g of the product of Step B in 15 ml of hot dioxane was cooled and 0.3 ml of hydrazine hydrate was added thereto. The mixture was stirred for 50 minutes at 20° C. and 7.5 ml of N hydrochloric acid were added thereto. The mixture was stirred for 15 hours and vacuum filtered. The filtrate was rinsed with water and the filtrate was evaporated to dryness to obtain 0.914 g of cis 4-thiocyanatomethyl-3-amino-2-oxo-azetidine hydrochloride.

후처리

  1. temperaturewas cooled
  2. stirringThe mixture was stirred for 15 hours
  3. filtrationvacuum filtered
  4. washThe filtrate was rinsed with water
  5. customthe filtrate was evaporated to dryness

출처 및 근거

ORD 기록
ord-22e4e9a0a5f4461485fc82d39aa8cd50
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05057512

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