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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 23030469, 화합물 → 4(3H)-Quinazolinone, 6-chloro-

HRID 1767153
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HRID 1767153 반응식
[Cl:1][C:2]1[CH:10]=[C:6]([C:7]([O-])=[O:8])[C:5]([NH2:11])=[CH:4][CH:3]=1.[NH4+:12].[CH:13]([O-])([O-])OC>CO>[Cl:1][C:2]1[CH:10]=[C:6]2[C:5](=[CH:4][CH:3]=1)[N:11]=[CH:13][NH:12][C:7]2=[O:8]
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참가 물질

4

반응물 2

HCID 23030469HCID 23030469, 화합물HCID 53629101Methylorthoformate

생성물 1

HCID 1354022734(3H)-Quinazolinone, 6-chloro-수율 94.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

In a 2-mL volume stainless steel pressure-resistant vessel were placed 340 mg (1.8 mmol) of ammonium 5-chloroanthranilate (prepared in the same manner as in Reference Example 3), 400 mg (3.6 mmol) of methyl orthoformate, and 1.5 mL of methanol. The reaction was carried out at 120° C. for 2 hours. After the reaction was complete, the reaction mixture was cooled to room temperature and analyzed (according to absolute quantitative analysis) by high performance liquid chromatography. There was produced 307 mg (reaction yield: 94%) of 6-chloroquinazolin-4-one.

후처리

  1. customIn a 2-mL volume stainless steel pressure-resistant vessel were placed

출처 및 근거

ORD 기록
ord-bede34a16338400a8019c875ab91dd49
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07232903B2

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