HCID 138051、化合物 → HCID 19922463、化合物

HRID 1681758ノート

反応式

HRID 1681758 の反応式
[S:1]1[CH:5]=[CH:4][C:3]2[CH2:6][C:7]3[C:12]([C:2]1=2)=[CH:11][CH:10]=[CH:9][CH:8]=3.C(C1SC=CC=1)=CC1C=CC=CC=1>>[S:1]1[CH:5]=[CH:4][C:3]2[C:6]3[CH:7]=[CH:8][CH:9]=[CH:10][C:11]=3[CH2:12][C:2]1=2

参加物

3

反応物 2

HCID 138051HCID 138051、化合物HCID 19922460HCID 19922460、化合物

生成物 1

HCID 19922463HCID 19922463、化合物

実験手順

The nitrogen in the above diazastilbenes and monoazastilbenes may be replaced with other heteroatoms and heterocycles to yield targets as shown in Scheme 71. ##STR91## For instance, 3-styrylthiophene (172) yields a photocyclization product (J. Chem. Soc. C, 2504 (1970) which may be converted by the methods described above to 4H-indeno[1,2-b]thiophene (173). Likewise, 2-styrylthiophene (175) is converted by photocyclization [J. Chem. Soc., 6221 (1965)] to an intermediate that will yield 8H-indeno[2,1-b]thiophene (176). These may then be alkylated by picolyl chloride to yield 4,4-bis(4-pyridinylmethyl)indeno[1,2-b]thiophene (174) and 8,8-bis(4-pyridinylmethyl)indeno[2,1-b]thiophene (177). Also, the furan derivatives are available via this route (Z. Naturfursch., Teil B, 24 (1969).

出典と根拠

ORDレコード
ord-13cb160d7df8417b8ffc78b52998e86a
出典データセット
uspto-grants-1992_12
特許番号
US05173489

反応ノート

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