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Water → HCID 178527906, 화합물

HRID 1597237
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HRID 1597237 반응식
[CH2:1]([O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13](=O)[NH:14][CH:15]=[N:16]2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:21].O>N1C=CC=CC=1>[CH2:1]([O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13](=[S:21])[NH:14][CH:15]=[N:16]2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14817Phosphorus sulfide (P2S5)HCID 1357631107-(Benzyloxy)-3,4-dihydroquinazolin-4-one

생성물 1

HCID 178527906HCID 178527906, 화합물수율 99%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A suspension of 7-benzyloxy-3,4-dihydroquinazolin-4-one (7 g, 28 mmol), (prepared as described for the starting material in Example 6), in pyridine (350 ml) containing phosphorus pentasulphide (12.5 g, 33 mmol) was heated at reflux for 8 hours. After cooling, the mixture was poured into water (1 liter). The precipitate was collected by filtration, and washed with water. The solid was dissolved in 6M sodium hydroxide and the solution was filtered. The filtrate was acidified to pH2 with 6M hydrochloric acid. The precipitate was collected by filtration, washed with water, and dried under vacuum at 60° C. to give 7-benzyloxy-3,4-dihydroquinazolin-4-thione (7.42 g, 99%).

후처리

  1. custom(prepared
  2. temperaturewas heated
  3. temperatureat reflux for 8 hours
  4. temperatureAfter cooling
  5. filtrationThe precipitate was collected by filtration
  6. washwashed with water
  7. dissolutionThe solid was dissolved in 6M sodium hydroxide
  8. filtrationthe solution was filtered
  9. filtrationThe precipitate was collected by filtration
  10. washwashed with water
  11. customdried under vacuum at 60° C.

출처 및 근거

ORD 기록
ord-81454e966c694571947f14c84503f8c9
출처 데이터셋
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06294532B1

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